# FDA Inspection 1011992 - Sonivate Medical, Inc. - May 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/sonivate-medical-inc/8e4e086d-90a8-4185-83b4-e40f415d1011
Source feed: FDA_Inspections

> FDA Inspection 1011992 for Sonivate Medical, Inc. on May 17, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1011992
- Company Name: Sonivate Medical, Inc.
- Inspection Date: 2017-05-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1011992 - 2017-05-17](https://www.keypedia.com/records/fda_inspections/sonivate-medical-inc/fb571671-68e5-4c58-af5d-6e7fa68ddd19)
- [FDA Inspection 863056 - 2014-01-23](https://www.keypedia.com/records/fda_inspections/sonivate-medical-inc/8f70a409-1696-4bb7-bc87-02c71875064f)
- [FDA Inspection 863056 - 2014-01-23](https://www.keypedia.com/records/fda_inspections/sonivate-medical-inc/5a5b3af8-5e80-4dba-9f78-cf63de10b01a)

Company: https://www.keypedia.com/companies/sonivate-medical-inc/5fb88415-b4d8-45f2-acef-a86011eea5ce

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7